ALDH1A2

Aldehyde dehydrogenase 1 family, member A2, also known as ALDH1A2 or retinaldehyde dehydrogenase 2 (RALDH2), is an enzyme that in humans is encoded by the ALDH1A2 gene.[5][6]

ALDH1A2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesALDH1A2, RALDH(II), RALDH2, RALDH2-T, aldehyde dehydrogenase 1 family member A2
External IDsOMIM: 603687 MGI: 107928 HomoloGene: 68368 GeneCards: ALDH1A2
Gene location (Human)
Chr.Chromosome 15 (human)[1]
Band15q21.3Start57,953,424 bp[1]
End58,497,866 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

8854

19378

Ensembl

ENSG00000128918

ENSMUSG00000013584

UniProt

O94788

Q62148

RefSeq (mRNA)

NM_170697
NM_001206897
NM_003888
NM_170696

NM_009022

RefSeq (protein)

NP_001193826
NP_003879
NP_733797
NP_733798

NP_033048

Location (UCSC)Chr 15: 57.95 – 58.5 MbChr 9: 71.22 – 71.3 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

This protein belongs to the aldehyde dehydrogenase family of proteins. The product of this gene is an enzyme that catalyzes the synthesis of retinoic acid (RA) from retinaldehyde. Retinoic acid, the active derivative of vitamin A (retinol), is a paracrine hormone signaling molecule that functions in developing and adult tissues.[7] The studies of a similar mouse gene suggest that this enzyme and the cytochrome CYP26A1, concurrently establish local embryonic retinoic acid levels that facilitate posterior organ development and prevent spina bifida. Three transcript variants encoding distinct isoforms have been identified for this gene.[6]

References

Further reading


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.